MGUS diet: Any tips on food to enjoy or prevent progression?
Hello-any tips on foods to avoid and foods to enjoy that help prevent progression of MGUS? I’ve read avoid radish, cherries, processed, fried. Focus more on fruits. Anyone adhered to special diet and have not had MGUS progress for years? Thank you, Susan
Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.
Hi Ginger, yes I have spent a lot of time reading posts :). I hope your myeloma treatment is going well. I think the renal considerations are going to be important for me too. I can see a slow rise in my creatinine and BUN - GFR still ok range.
Nor did my hematologist mention anything about diet with myeloma and kidney issues
Any with MM also have active Mastocytosis? Bone marrow show both.
Hi Wyom1998, welcome to Mayo Clinic Connect. You asked to connect with someone who has both multiple myeloma and mastocytosis. I think @megansims might.
Wyom, is this a new diagnosis for you?
Marrow biopsies found at the same time in May
What treatment plan has been suggested for you? What are your next steps?
RVD weekly on 28 day cycles x 4 then transplant for MM in December.
I am frustrated nothing is addressed for mastocytosis. I think those symptoms are worth treatment, but doctor says no. BP sits around 98/55. Seems low to me.
Do any of you have afib and MGUS. I am wondering if afib meds caused blood disorder??
Has anyone had MGUS discovered after taking the COVID vaccine?
Hi Deryl, welcome to Mayo Clinic Connect. You'll notice that I moved your question to the Blood Cancers & Disorders group. I did this because you'll find members talking about MGUS in this group and can connect with people like @gingerw @auntieoakley @anniemaggie @susangs @momofthree1 @gmajudy @cctoo @dazlin
Here are a couple of other discussions that may interest you.
- Always run down with MGUS: https://connect.mayoclinic.org/discussion/always-run-down-with-mgus/
- MGUS https://connect.mayoclinic.org/discussion/mgus-2d464e/
I see that you are looking for a cause for your recent MGUS diagnosis and ask about the vaccine or a-fib meds being the potential culprit. The precise cause of MGUS isn't known. Genetic changes and environmental triggers appear to play a role. It may be a frustrating pursuit to seek the cause. By connecting with others here, I hope that you can turn your focus and energies to coping with the diagnosis and staying healthy.
What questions do you have? Has your doctor set up a follow-up schedule? How frequent?